Differential Distribution of GABA and GAT1 in Mouse Epididymis

Zhang Wenping1#, Qi Lixin2#, Le Wei2, Hu Jiahua3, Lihe Guo3, Huai L Feng4 and Zhang Jinfu5*

1Department of Dermatology, Tongji Hospital, Tongji University School of Medicine, Shanghai, P.R. China

2Department of Urology, Tongji Hospital, Tongji University School of Medicine, Shanghai, P.R. China

3Department of Molecular Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, P.R. China

4Department of Obstetrics and Gynecology, New York Hospital Queens affiliated Weill Medical College of Cornell University, New York, USA

5Department of Urology, Shanghai Tongren Hospital, Shanghai, P.R. China

#Equal Contribution

*Corresponding Author:
Zhang Jinfu
Department of Urology, Shanghai Tongren Hospital
1111 Xianxia Road, Shanghai, 200336, P.R. China
Tel: 086-21-62909915
E-mail: zhangjinfu@tongji.edu.cn

Received Date: October 28, 2017; Accepted Date: November 15, 2017; Published Date: November 20, 2017

Citation: Wenping Z, Lixin Q, Wei L, Jiahua H, Gua L, et al. (2017) Differential Distribution of GABA and GAT1 in Mouse Epididymis. Ann Clin Lab Res Vol.5: No.4:203. DOI: 10.21767/2386-5180.1000203

 
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Abstract

The present study is to explore the relationship between GABA/GAT1 and mechanism of sperm maturation in epididymis. The distribution of GABA and GAT1 was observed under microscope in different magnifications. Immune labeled GABA and GAT1 at the different regions of epididymis was semi-quantified. Our data illustrated that GABA was significantly higher produced at caput of epididymis than that at corpus or cauda of epididymis. Consistently, the distribution of GAT1 showed similar patterns at the different regions of epididymis. The current data suggested that differential expression of GABA and its transport protein I (GAT1) at the different regions of epididymis may be related to maturation and subsequently the function of sperms. Such information may also contribute to our clinical practice in Andrology.

Keywords

Immunohistochemistry; Epididymis; GABA; GAT1

Abbreviations

GABA: γ-Aminobutyric Acid; GAT1: GABA Transport Protein I

Introduction

γ-aminobutyric acid (GABA) is a main inhibitory neurotransmitter in the mammalian central nervous system [1]. Neuronal inhibition is induced following GABA binding with ionic GABAA/GABAC receptor and metabolic GABAB receptor of postsynaptic membrane. GAT1 is a primary neuron transporter in brain among the four GATs (GAT1-GAT4) [2,3]. Synaptic transmission is terminated by GABA transporter protein (GAT) reuptaking GABA. In addition to localization in CNS, GABA is also identified in peripheral tissues [4], such as endocrine organs (pituitary, liver and ovary). It has been published previously that GABA is also presented in testis, sperm, deferent duct and epididymis in male reproductive system [5]. However the distribution of GABA and GAT1 in epididymis is still not clear. Similar to progesterone, GABA causes depolarization of cell membrane and stimulates acrosome reactions in recapacitated human spermatozoa in a dose dependent manner [6]. GABAA and GABAB receptors, expressed in sperms, might relate to acrosome reaction via GABA and progesterone [7-11]. GABA also enhances sperm kinematic parameters and increases hyper-activation, with similar magnitude of those produced by progesterone and mediated mainly by the GABAA receptor [12]. Thus GABA may be a physiological regulator of sperm function. GAT1 is also observed in testes, epididymis and sperms [13-18]. The function of GAT1 has been demonstrated, showing compromised reproductive capacity in the GAT1 transgenic mice. The explanation of compromised reproduction of the GAT1 transgenic mice may be due to disturbed maturation of sperms, compared with wild type mice [15]. Therefore it is necessary to determine the distribution and/or correlation of GABA and GAT1 in epididymis, which may shed light in the role of these molecules in the maturation of sperm, which could be useful for understanding of male infertility with potential application in the management of such patients.

Materials and Methods

Animals

Adult C57 mice (n=4) (aged 8 weeks) were kept at the standard condition, as described [19]. Temperature of 22±2 and diurnal cycle of 12 hours were maintained. All experimental protocols were approved by Animal Ethic Committee, Tongji Hospital, Tongji University School of Medicine.

Histology

Epididymis was collected following cervical dislocation sacrificing. The collected epididymis was fixed with 4% paraformaldehyde and embedded in paraffin. Paraffin-sections (7 μm) were cut using Leica microtome. The sections were blocked with the rabbit serum-free protein following dewaxing. GABA and GAT1 antibodies were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Sections were incubated with either primary anti-GABA or anti-GAT1 (1:50) overnight at 4. These sections were further incubated with the secondary m (biotinylated rabbit anti-goat IgG) at room temperature after three times PBS washing. The sections were incubated with the horseradish peroxidase-labeled streptavidin for 30 min (goat sreptavidin/peroxidase Kit-SP 9003, Zhongshan Goldenbridge Biotechnology, Co LTD, China). Detection was performed with the AEC substrate. The color development was stopped using washing the slides with running water. Finally, sections were counterstained with hematoxylin. The controls were performed by omitting the primary antibody. The slides were then photographed under Leica microscope. Semi-quantification of the immunohistochemistry was performed using Axioplan 2 image microscopic image analysis system (Zeiss Company, Germany).

Statistical analysis

SPSS13.0 was used for the statistical analyses. Data are presented as mean±SD. Comparisons were made using t test. p<0.05 was considered statistically significant.

Results

GABA and GAT1 immunohistochemistry in epididymis

There was overall GABA production in the whole epididymis, including caput, corpus, and cauda (Figure 1a). However, GABA production in caput (Figure 1b) was 1.7 or 1.6-fold stronger than that in corpus or cauda, respectively (Figures 1c and 1d). Interestingly there was no significant difference of GABA between corpus and cauda. Similarly, GAT1 was also distributed in the whole epididymis, with similar patterns to that of GABA (Figures 2a-2d). The control showed no special staining (Figures 3a-3d).

Annals-Clinical-Laboratory-GABA-epididymis

Figure 1: Immunohistochemistry of GABA in epididymis. (a) GABA staining over the epididymis (x40); (b) Epididymis caput (x400); (c) Epididymis corpus (x400); (d) Epididymis cauda (x400).

Annals-Clinical-Laboratory-GAT1-epididymis

Figure 2: Immunohistochemistry of GAT1 in epididymis of C57 mice. (a) GAT1 staining over the epididymis (x40); (b) Epididymis caput (x400); (c) Epididymis corpus (x400); (d) Epididymis cauda (x400).

Annals-Clinical-Laboratory-immunohistochemistry-epididymis

Figure 3: Control of immunohistochemistry in epididymis of C57 mice. (a) The whole epididymis (x40); Epididymis caput (x400); (c) Epididymis corpus (x400); (d) Epididymis cauda (x400).

Semiquantification of immunohistochemistry staining intensity of GABA and GAT1

The intensity of GABA staining varied from the caput 95.5 ± 6.5 to the corpus 55.9 ± 3.5 and the cauda 59.2 ± 4.2. The intensity of GAT1 varied from the caput 75.3 ± 2.0 to the corpus 52.0 ± 2.9 and the cauda 54.5 ± 1.7. The results identified that GABA distributed significantly (p<0.01) in the caput of epididymis, instead of the corpus and cauda. GAT1 has the similar distribution pattern as GABA (Figures 4a and 4b).

Annals-Clinical-Laboratory-semi-quantification

Figure 4: The immunohistochemistry semi-quantification results. Values were mean±SD. (a) GABA production in mouse epididymis; (b) GAT1 production in mouse epididymis. ** indicates p<0.01.

Discussion

GABA (expressed in sperms, testes and epididymis) plays an important role in spermiotelcosis [13-15]. Our previous studies demonstrate that there are abnormal histopathological presentations in testis and sperm from GAT1 transgenic mice. However, there are no remarkable changes in the epididymis [15]. This can explain that the male reproduction is compromised in GAT1 transgenic mice [15,16]. In the current study, we found that GABA and GAT1 distributed differentially in mouse epididymis caput, corpus, and cauda. Our current findings are in line with our previous two reports, showing that there was differential distribution of GABA, as well as, GAT1 in epididymis, particularly in caput, suggesting that GABA and GAT1 may contribute to the maturation of sperm and reproduction in male.

GAT1 is responsible for transferring GABA from the epididymis lumen into the epithelium cells for homeostasis in epididymis. Consistent distribution of GABA and GAT1 in epididymis caput, corpus, and cauda, might be due to that GAT1 regulates concentration of GABA in the epididymis [15].

The physiological function of epididymis is mainly for sperm maturation. Spermatozoa enter the epididymal tubule from the testis and, undergo a process of maturation that confers motility and the ability to fertilize ova during transit [18]. GABA is able to induce sperm acrosome reaction and increase sperm motility in vitro [7,10,12]. Acrosome reaction is a critical step for fertilization; whereas motility is also important for sperms to reach ova for fertilization. Thus the highest production of GABA/GAT1 in the epididymis caput is consistent with our previous published work, suggesting that GABA contributes to both acrosome reaction and sperm motility.

Conclusion

To conclude, our observation suggests that GABA and GAT1 play an important role in epididymal function. Such information is important for basic research in reproductive physiology, as well as, for clinical practice in Andrology.

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